A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117839



Internal ID21301105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:155013502..155038534hg38UCSC Ensembl
Innerchr6:155334636..155359668hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3825033
hg1925033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083114
Samplessample364
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117839
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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